A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070592



Internal ID19319651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61961466..61962767hg38UCSC Ensembl
chr13:62535599..62536900hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772360
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070592
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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